Central Laboratory, Xuanwu Hospital of Capital Medical University, Key Laboratory for Neurodegenerative Disease of Ministry of Education, #45 Changchun Street, Xuanwu District, Beijing 100053, China.
Neurosci Lett. 2010 Jan 14;468(3):173-7. doi: 10.1016/j.neulet.2009.07.058. Epub 2009 Jul 24.
Amyloid precursor protein 17-mer peptide (APP 17-mer peptide) is an active fragment of amyloid precursor protein (APP) in the nervous system that mediates various neuronal activities and functions. Estrogen deprivation during menopause disproportionately increases the risk of many neurodegenerative diseases, including Alzheimer's disease (AD). Currently, therapeutic approaches to treat Alzheimer's disease are less than effective. We have previously shown that APP 17-mer peptide participates in neuronal function in aged-hippocampal neurons. In this study, we investigate the effects of estrogen and APP 17-mer peptide on hippocampal neurodegeneration in ovariectomized rats. The results showed that decreases in learning and memory function in ovariectomized rats were associated with degenerative changes in hippocampal neurons. Estrogen deprivation also enhances apoptotic cell death and decreases expression of the anti-apoptotic protein Bcl-2. Administration of APP 17-mer peptide ameliorates changes associated with estrogen deprivation without affecting estrogen levels. These results indicate that APP 17-mer peptide may prevent neurodegeneration caused by estrogen deficiency. Our findings also suggest that estrogen deficiency-induced neurodegeneration is regulated by activation of an intracellular "cross talk" signaling pathway, connecting neurotrophins with APP 17-mer peptide.
淀粉样前体蛋白 17 肽(APP 17 肽)是神经系统中淀粉样前体蛋白(APP)的活性片段,介导各种神经元活动和功能。绝经期雌激素缺乏不成比例地增加了许多神经退行性疾病的风险,包括阿尔茨海默病(AD)。目前,治疗阿尔茨海默病的方法效果不佳。我们之前已经表明,APP 17 肽参与老年海马神经元的神经元功能。在这项研究中,我们研究了雌激素和 APP 17 肽对去卵巢大鼠海马神经退行性变的影响。结果表明,去卵巢大鼠学习和记忆功能的下降与海马神经元的退行性变化有关。雌激素剥夺还增强了细胞凋亡和降低了抗凋亡蛋白 Bcl-2 的表达。APP 17 肽的给药改善了与雌激素剥夺相关的变化,而不影响雌激素水平。这些结果表明,APP 17 肽可能预防由雌激素缺乏引起的神经退行性变。我们的研究结果还表明,雌激素缺乏诱导的神经退行性变是由细胞内“串扰”信号通路的激活调节的,该通路将神经营养因子与 APP 17 肽连接起来。